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Efficacy of Sprint Interval Training on Anthropometric Measures

Effectiveness of Sprint Interval Training on Anthropometric Measures Among Obese and Overweight Young Adults: A Systematic Review

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04323995
Enrollment
500
Registered
2020-03-27
Start date
2020-03-02
Completion date
2021-02-05
Last updated
2021-06-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Overweight and Obesity

Brief summary

Due to the rising problem of overweight and obesity, many strategies are implemented to combat this issue and one of the most common ways is exercise training. Aerobic exercise is a popular and effective conservative strategy for weight and adiposity management and commonly used exercise protocols are moderate-intensity continuous training (MICT) and interval training (IT). MICT is typically defined as continuous effort that elicits 55%-70% of the maximal heart rate or promotes oxygen consumption equivalent to 40%-60% of the maximum oxygen intake. IT involves repeated exercise with periods of recovery, which includes high intensity interval training (HIIT) and Sprint interval training (SIT). HIIT is exercising at 80% to 100% of maximal heart rate while SIT involves all-out or supramaximal effort at the intensity of 100% of maximal oxygen uptake. Multiple systematic reviews on the effect of SIT on aerobic capacity or comparisons between other forms of exercise protocols to reduce body adiposity has been conducted, but so far no systematic review has been carried out to evaluate the efficacy of this protocol solely on anthropometric measures on young obese and overweight adults alone. Hence, in this study, a systematic review of the effect of SIT on anthropometric measurements in young obese or overweight adults will be reviewed, filtered and assembled.

Detailed description

Keywords using obese, overweight, sprint interval training, interval training, anthropometric measures,body mass index, fat % lean muscle mass will be searched through e-databases namely Pubmed (including MEDLINE), Pedro-search, Science Direct, Google Scholar, Web of Science, Scopus and Cochrane Library for the suitable original full text studies. Only randomized control trails will be included in this study and the Tool for the assEssment of Study qualiTy and reporting in EXercise (TESTEX) would be utilized to assess each individual study. TESTEX has been validated and is specific to exercise training. The authors wish to use TESTEX as it addresses several shortcomings that PEDro does not e.g. exercise adherence, withdrawal, relative exercise training intensity. In addition, study quality assessment of training studies is more robust with TESTEX. 2 independent evaluators will examine and screen each study for its efficacy to be included in the data analysis.

Interventions

Sprint interval training of 2 weeks and more.

Sponsors

Universiti Tunku Abdul Rahman
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Male and female individuals aged 18-35 years old * Overweight individuals with a BMI of 25.0 to \<30 * Obese individuals with a BMI of 30.0 or higher * Original full texts with SIT as intervention, occurring 2 weeks or more

Exclusion criteria

* Male and female individuals aged below 18 and above 35 years old * SIT as intervention, occurring less than 2 weeks

Design outcomes

Primary

MeasureTime frame
BMI for changeAt baseline (before intervention begin) and post training.
Fat % for changeAt baseline (before intervention begin) and post training.
Lean Muscle MassAt baseline (before intervention begin) and post training.
Waist Circumference for changeAt baseline (before intervention begin) and post training.
Waist to hip ratio for changeAt baseline (before intervention begin) and post training.

Countries

Malaysia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026